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miRNA as a Modulator of Immunotherapy and Immune Response in Melanoma

Immune checkpoint inhibitors are a promising therapy for the treatment of cancers, including melanoma, that improved benefit clinical outcomes. However, a subset of melanoma patients do not respond or acquire resistance to immunotherapy, which limits their clinical applicability. Recent studies have...

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Autores principales: Nguyen, Mai-Huong Thi, Luo, Yueh-Hsia, Li, An-Lun, Tsai, Jen-Chieh, Wu, Kun-Lin, Chung, Pei-Jung, Ma, Nianhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615556/
https://www.ncbi.nlm.nih.gov/pubmed/34827646
http://dx.doi.org/10.3390/biom11111648
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author Nguyen, Mai-Huong Thi
Luo, Yueh-Hsia
Li, An-Lun
Tsai, Jen-Chieh
Wu, Kun-Lin
Chung, Pei-Jung
Ma, Nianhan
author_facet Nguyen, Mai-Huong Thi
Luo, Yueh-Hsia
Li, An-Lun
Tsai, Jen-Chieh
Wu, Kun-Lin
Chung, Pei-Jung
Ma, Nianhan
author_sort Nguyen, Mai-Huong Thi
collection PubMed
description Immune checkpoint inhibitors are a promising therapy for the treatment of cancers, including melanoma, that improved benefit clinical outcomes. However, a subset of melanoma patients do not respond or acquire resistance to immunotherapy, which limits their clinical applicability. Recent studies have explored the reasons related to the resistance of melanoma to immune checkpoint inhibitors. Of note, miRNAs are the regulators of not only cancer progression but also of the response between cancer cells and immune cells. Investigation of miRNA functions within the tumor microenvironment have suggested that miRNAs could be considered as key partners in immunotherapy. Here, we reviewed the known mechanism by which melanoma induces resistance to immunotherapy and the role of miRNAs in immune responses and the microenvironment.
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spelling pubmed-86155562021-11-26 miRNA as a Modulator of Immunotherapy and Immune Response in Melanoma Nguyen, Mai-Huong Thi Luo, Yueh-Hsia Li, An-Lun Tsai, Jen-Chieh Wu, Kun-Lin Chung, Pei-Jung Ma, Nianhan Biomolecules Review Immune checkpoint inhibitors are a promising therapy for the treatment of cancers, including melanoma, that improved benefit clinical outcomes. However, a subset of melanoma patients do not respond or acquire resistance to immunotherapy, which limits their clinical applicability. Recent studies have explored the reasons related to the resistance of melanoma to immune checkpoint inhibitors. Of note, miRNAs are the regulators of not only cancer progression but also of the response between cancer cells and immune cells. Investigation of miRNA functions within the tumor microenvironment have suggested that miRNAs could be considered as key partners in immunotherapy. Here, we reviewed the known mechanism by which melanoma induces resistance to immunotherapy and the role of miRNAs in immune responses and the microenvironment. MDPI 2021-11-08 /pmc/articles/PMC8615556/ /pubmed/34827646 http://dx.doi.org/10.3390/biom11111648 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Nguyen, Mai-Huong Thi
Luo, Yueh-Hsia
Li, An-Lun
Tsai, Jen-Chieh
Wu, Kun-Lin
Chung, Pei-Jung
Ma, Nianhan
miRNA as a Modulator of Immunotherapy and Immune Response in Melanoma
title miRNA as a Modulator of Immunotherapy and Immune Response in Melanoma
title_full miRNA as a Modulator of Immunotherapy and Immune Response in Melanoma
title_fullStr miRNA as a Modulator of Immunotherapy and Immune Response in Melanoma
title_full_unstemmed miRNA as a Modulator of Immunotherapy and Immune Response in Melanoma
title_short miRNA as a Modulator of Immunotherapy and Immune Response in Melanoma
title_sort mirna as a modulator of immunotherapy and immune response in melanoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615556/
https://www.ncbi.nlm.nih.gov/pubmed/34827646
http://dx.doi.org/10.3390/biom11111648
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